Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23433619G>A | CA027761 | MYH7 | c.114C>T (p.Phe38=) n.220C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23433619G>C | CA389053860 | MYH7 | c.114C>G (p.Phe38Leu) n.220C>G | |
14 | g.23433619G= | CA2123455882 | MYH7 | c.114C= (p.Phe38=) n.220C= | |
14 | g.23433619G>T | CA389053861 | MYH7 | c.114C>A (p.Phe38Leu) n.220C>A | |
14 | g.23433620A>C | CA389053863 | MYH7 | c.113T>G (p.Phe38Cys) n.219T>G | |
14 | g.23433620A>G | CA389053866 | MYH7 | c.113T>C (p.Phe38Ser) n.219T>C | ClinVar |
14 | g.23433620A>T | CA389053864 | MYH7 | c.113T>A (p.Phe38Tyr) n.219T>A | |
14 | g.23433621A= | CA2123455885 | MYH7 | c.112T= (p.Phe38=) n.218T= | |
14 | g.23433621A>C | CA389053867 | MYH7 | c.112T>G (p.Phe38Val) n.218T>G | |
14 | g.23433621A>G | CA389053869 | MYH7 | c.112T>C (p.Phe38Leu) n.218T>C | dbSNP gnomAD v3 gnomAD v4 |
14 | g.23433621A>T | CA389053871 | MYH7 | c.112T>A (p.Phe38Ile) n.218T>A | |
14 | g.23433622G>A | CA485627144 | MYH7 | c.111C>T (p.Val37=) n.217C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.23433622G>C | CA485627145 | MYH7 | c.111C>G (p.Val37=) n.217C>G | |
14 | g.23433622G= | CA2123455886 | MYH7 | c.111C= (p.Val37=) n.217C= | |
14 | g.23433622G>T | CA485627146 | MYH7 | c.111C>A (p.Val37=) n.217C>A | COSMIC |
14 | g.23433623A>C | CA389053872 | MYH7 | c.110T>G (p.Val37Gly) n.216T>G | |
14 | g.23433623A>G | CA389053873 | MYH7 | c.110T>C (p.Val37Ala) n.216T>C | |
14 | g.23433623A>T | CA389053875 | MYH7 | c.110T>A (p.Val37Asp) n.216T>A | |
14 | g.23433624C>A | CA389053877 | MYH7 | c.109G>T (p.Val37Phe) n.215G>T | |
14 | g.23433624C>G | CA389053879 | MYH7 | c.109G>C (p.Val37Leu) n.215G>C | |
14 | g.23433624C>T | CA389053880 | MYH7 | c.109G>A (p.Val37Ile) n.215G>A | ClinVar |
14 | g.23433625A>C | CA389053881 | MYH7 | c.108T>G (p.Asp36Glu) n.214T>G | |
14 | g.23433625A>G | CA485627147 | MYH7 | c.108T>C (p.Asp36=) n.214T>C | dbSNP |
14 | g.23433625A>T | CA389053883 | MYH7 | c.108T>A (p.Asp36Glu) n.214T>A | |
14 | g.23433626T>A | CA389053888 | MYH7 | c.107A>T (p.Asp36Val) n.213A>T | dbSNP gnomAD v4 |
14 | g.23433626T>C | CA389053887 | MYH7 | c.107A>G (p.Asp36Gly) n.213A>G | |
14 | g.23433626T>G | CA389053885 | MYH7 | c.107A>C (p.Asp36Ala) n.213A>C | gnomAD v4 |
14 | g.23433626T= | CA2123455887 | MYH7 | c.107A= (p.Asp36=) n.213A= | |
14 | g.23433627C>A | CA389053890 | MYH7 | c.106G>T (p.Asp36Tyr) n.212G>T | |
14 | g.23433627C>G | CA389053893 | MYH7 | c.106G>C (p.Asp36His) n.212G>C | |
14 | g.23433627C>T | CA389053892 | MYH7 | c.106G>A (p.Asp36Asn) n.212G>A | |
14 | g.23433628C>A | CA389053894 | MYH7 | c.105G>T (p.Lys35Asn) n.211G>T | |
14 | g.23433628C= | CA2123455890 | MYH7 | c.105G= (p.Lys35=) n.211G= | |
14 | g.23433628C>G | CA389053895 | MYH7 | c.105G>C (p.Lys35Asn) n.211G>C | |
14 | g.23433628C>T | CA027479 | MYH7 | c.105G>A (p.Lys35=) n.211G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23433629T>A | CA389053897 | MYH7 | c.104A>T (p.Lys35Met) n.210A>T | |
14 | g.23433629T>C | CA389053899 | MYH7 | c.104A>G (p.Lys35Arg) n.210A>G | |
14 | g.23433629T>G | CA389053900 | MYH7 | c.104A>C (p.Lys35Thr) n.210A>C | |
14 | g.23433630T>A | CA389053902 | MYH7 | c.103A>T (p.Lys35Ter) n.209A>T | |
14 | g.23433630T>C | CA389053904 | MYH7 | c.103A>G (p.Lys35Glu) n.209A>G | gnomAD v4 |
14 | g.23433630T>G | CA389053905 | MYH7 | c.103A>C (p.Lys35Gln) n.209A>C | |
14 | g.23433631C>A | CA389053907 | MYH7 | c.102G>T (p.Lys34Asn) n.208G>T | |
14 | g.23433631C>G | CA389053908 | MYH7 | c.102G>C (p.Lys34Asn) n.208G>C | |
14 | g.23433631C>T | CA485627148 | MYH7 | c.102G>A (p.Lys34=) n.208G>A | |
14 | g.23433632T>A | CA389053913 | MYH7 | c.101A>T (p.Lys34Met) n.207A>T | |
14 | g.23433632T>C | CA389053911 | MYH7 | c.101A>G (p.Lys34Arg) n.207A>G | dbSNP |
14 | g.23433632T>G | CA389053909 | MYH7 | c.101A>C (p.Lys34Thr) n.207A>C | |
14 | g.23433633T>A | CA389053914 | MYH7 | c.100A>T (p.Lys34Ter) n.206A>T | |
14 | g.23433633T>C | CA389053915 | MYH7 | c.100A>G (p.Lys34Glu) n.206A>G | |
14 | g.23433633T>G | CA389053916 | MYH7 | c.100A>C (p.Lys34Gln) n.206A>C |